Full metadata
Title
Generalized linear models in Bayesian phylogeography
Description
Bayesian phylogeography is a framework that has enabled researchers to model the spatiotemporal diffusion of pathogens. In general, the framework assumes that discrete geographic sampling traits follow a continuous-time Markov chain process along the branches of an unknown phylogeny that is informed through nucleotide sequence data. Recently, this framework has been extended to model the transition rate matrix between discrete states as a generalized linear model (GLM) of predictors of interest to the pathogen. In this dissertation, I focus on these GLMs and describe their capabilities, limitations, and introduce a pipeline that may enable more researchers to utilize this framework.
I first demonstrate how a GLM can be employed and how the support for the predictors can be measured using influenza A/H5N1 in Egypt as an example. Secondly, I compare the GLM framework to two alternative frameworks of Bayesian phylogeography: one that uses an advanced computational technique and one that does not. For this assessment, I model the diffusion of influenza A/H3N2 in the United States during the 2014-15 flu season with five methods encapsulated by the three frameworks. I summarize metrics of the phylogenies created by each and demonstrate their reproducibility by performing analyses on several random sequence samples under a variety of population growth scenarios. Next, I demonstrate how discretization of the location trait for a given sequence set can influence phylogenies and support for predictors. That is, I perform several GLM analyses on a set of sequences and change how the sequences are pooled, then show how aggregating predictors at four levels of spatial resolution will alter posterior support. Finally, I provide a solution for researchers that wish to use the GLM framework but may be deterred by the tedious file-manipulation requirements that must be completed to do so. My pipeline, which is publicly available, should alleviate concerns pertaining to the difficulty and time-consuming nature of creating the files necessary to perform GLM analyses. This dissertation expands the knowledge of Bayesian phylogeographic GLMs and will facilitate the use of this framework, which may ultimately reveal the variables that drive the spread of pathogens.
I first demonstrate how a GLM can be employed and how the support for the predictors can be measured using influenza A/H5N1 in Egypt as an example. Secondly, I compare the GLM framework to two alternative frameworks of Bayesian phylogeography: one that uses an advanced computational technique and one that does not. For this assessment, I model the diffusion of influenza A/H3N2 in the United States during the 2014-15 flu season with five methods encapsulated by the three frameworks. I summarize metrics of the phylogenies created by each and demonstrate their reproducibility by performing analyses on several random sequence samples under a variety of population growth scenarios. Next, I demonstrate how discretization of the location trait for a given sequence set can influence phylogenies and support for predictors. That is, I perform several GLM analyses on a set of sequences and change how the sequences are pooled, then show how aggregating predictors at four levels of spatial resolution will alter posterior support. Finally, I provide a solution for researchers that wish to use the GLM framework but may be deterred by the tedious file-manipulation requirements that must be completed to do so. My pipeline, which is publicly available, should alleviate concerns pertaining to the difficulty and time-consuming nature of creating the files necessary to perform GLM analyses. This dissertation expands the knowledge of Bayesian phylogeographic GLMs and will facilitate the use of this framework, which may ultimately reveal the variables that drive the spread of pathogens.
Date Created
2017
Contributors
- Magee, Daniel (Author)
- Scotch, Matthew L (Thesis advisor)
- Gonzalez, Graciela H (Committee member)
- Taylor, Jesse E (Committee member)
- Arizona State University (Publisher)
Topical Subject
Resource Type
Extent
ix, 141 pages : illustrations (some color), color maps
Language
eng
Copyright Statement
In Copyright
Primary Member of
Peer-reviewed
No
Open Access
No
Handle
https://hdl.handle.net/2286/R.I.43917
Statement of Responsibility
by Daniel Magee
Description Source
Retrieved on July 11, 2017
Level of coding
full
Note
thesis
Partial requirement for: Ph.D., Arizona State University, 2017
bibliography
Includes bibliographical references (pages 109-117)
Field of study: Biomedical informatics
System Created
- 2017-06-01 01:02:28
System Modified
- 2021-08-30 01:19:38
- 3 years 2 months ago
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